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Applied and Environmental Soil Science
Volume 2012 (2012), Article ID 632172, 9 pages
http://dx.doi.org/10.1155/2012/632172
Research Article

Suppression of Bromus tectorum L. by Established Perennial Grasses: Potential Mechanisms—Part One

USDA-Agricultural Research Service, Great Basin Rangelands Research Unit, 920 Valley Road, Reno, NV 89512, USA

Received 29 March 2012; Revised 30 May 2012; Accepted 6 June 2012

Academic Editor: D. L. Jones

Copyright © 2012 Robert R. Blank and Tye Morgan. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Bromus tectorum L. (cheatgrass) is an Eurasian annual grass that has invaded ecosystems throughout the Intermountain west of the United States. Our purpose was to examine mechanisms by which established perennial grasses suppress the growth of B. tectorum. Using rhizotrons, the experiment was conducted over 5 growth cycles: (1) B. tectorum planted between perennial grasses; (2) perennials clipped and B. tectorum planted; (3) perennials clipped and B. tectorum planted into soil mixed with activated carbon; (4) perennials clipped, B. tectorum planted, and top-dressed with fertilizer, and; (5) perennial grasses killed and B. tectorum planted. Water was not limiting in this study. Response variables measured at the end of each growth cycle included above-ground mass and tissue nutrient concentrations. Relative to controls (B. tectorum without competition), established perennial grasses significantly hindered the growth of B. tectorum. Overall, biomass of B. tectorum, grown between established perennials, increased considerably after fertilizer addition and dramatically upon death of the perennials. Potential mechanisms involved in the suppression of B. tectorum include reduced nitrogen (possibly phosphorus) availability and coopting of biological soil space by perennial roots. Our data cannot confirm or reject allelopathic suppression. Understanding the mechanisms involved with suppression may lead to novel control strategies against B. tectorum.

1. Introduction

The Eurasian annual grass B. tectorum L. (cheatgrass, downy brome) has come to dominate many ecosystems in the Intermountain Region of the Western United States [1]. Pathways by which B. tectorum facilitate its expansion are myriad and include phenotypic plasticity to new host environments [2], it increases the rates and sizes of wildfires, which fosters more invasion [3], rapid above-and below-ground growth rates [4, 5], prolific seed production [6], landscape disturbance [79], and elevated atmospheric CO2 [10, 11].

Given the invasion success of B. tectorum, one might conclude that it is competitive. In the seedling stage, B. tectorum is quite competitive against native and introduced perennial grasses [1214]. Particular ecosystems, however, are resistant to invasion by B. tectorum [15]. A common thread in ecosystem resistance to B. tectorum invasion is healthy, well-established, perennial grass communities such as the natives Pesudoroegneria spicata (bluebunch wheatgrass), Elymus elymoides (bottlebrush squirreltail), Poa secunda (bluegrass), and Festuca idahoensis (Idaho fescue), and the introduced Eurasian Agropyron cristatum (crested wheatgrass) [1618]. Established perennial grasses that grow early in the spring and maintain growth during the winter have been shown to suppress annual weeds [19]. By what mechanisms do these perennial grass communities resist B. tectorum invasion? Very meager literature exists on specific mechanisms of plant suppression. In the framework of ecological resistance theory [20], what factors in a host environment populated by healthy perennial grasses might constrain the invasiveness of B. tectorum?

The biotic and abiotic factors that influence community resistance can work in synergism making it difficult to decipher-specific mechanisms. In the case of B. tectorum, empirical evidence implicates soil resource availability, particularly nitrogen and phosphorus, as an important candidate mechanism [16, 17, 21, 22]. Addition of nitrogen fertilizer greatly increases the growth and competitive stature of B. tectorum [23, 24]. Conversely, immobilization of mineral soil nitrogen via the addition of a labile carbon source can greatly reduce populations of B. tectorum [25, 26], although factors other than nitrogen immobilization may be partially responsible [27]. We ask the question: do healthy perennial grass communities, through a network of established perennial roots, control soil nutrient availability at a low level such that B. tectorum is less successful [28]?

Resistance to plant invasion via root competition can manifest itself in mechanisms other than decreasing nutrient availability [29]. The concept of biological soil space has relevance here. One aspect of biological soil space is that it provides an open niche that plant roots can exploit and indeed is necessary for plants to establish [30]. Another aspect is that the physical space, itself, may also be a soil resource [31]. The mechanistic underpinnings of how physical space influences plant growth are speculative, but it is suggested that flexibility to deploy roots to fragmented areas of physical space may confer greater ability to access soil nutrients [32]. If physical soil space is a resource, then a plant root that occupies that soil space must reduce the utility of that space to a competing root. Indeed the chemical and biological environment near-established perennial roots may negatively affect the roots of potential plant invaders. Some invasive species exude allelopathies to gain a competitive advantage in their new host environments [33, 34]. Conversely, some native plants resist invasion by producing allelopathies [35, 36]. We ask another question: do healthy perennial grasses resist B. tectorum invasion by coopting biological soil space or by possibly exuding allelopathies?

This study was designed to test if and by what mechanisms established perennial grasses suppress B. tectorum. Our approach was to use multiple growth cycles to evaluate different aspects of suppression including declining soil nutrient resources, allelopathy, root competition, supplemental soil nutrients, and finally death of the perennial grasses. The working hypotheses posit that (1) established perennial grasses will suppress the growth of B. tectorum; (2) established perennial grasses will control soil nutrients, particularly nitrogen, to levels low enough such that growth of B. tectorum is reduced; (3) established perennial grass roots will occupy biological soil space and/or exude allelopathies thus causing reduction in the growth potential of B. tectorum.

2. Materials and Methods

The experiment was conducted in a greenhouse at Reno, NV, USA (39°32′17.20′′N; 119°48′22.89′′W). The soil substrate was freshly collected from a Krascheninnikovia lanata (winterfat) site, invaded by B. tectorum L. for about 10 years, about 80 km northwest of Reno, NV, USA. Surface soil (0–25 cm, corresponding to the A horizon) was composited from an area of about 10 m2. The soil, loamy sand in texture, was sieved to remove coarse fragments and medium-to-large roots and homogenized by hand mixing on a greenhouse bench. Replicate clear plastic rhizotrons, 5 × 30 × 100 cm depth, were filled with equal volume of the soil. The outsides of the rhizotrons were covered with insulation that could be removed from the back to observe rooting patterns. Prior to seed planting, rhizotrons were paired in adjoining plastic containers to maintain a slight angle so that roots would readily intercept the clear rhizotron backing for observation, and the soil was saturated with deionized water. The competitive effect of three established native perennial grasses against B. tectorum was tested. Elymus wawawaiensis (Snake River wheatgrass) is a long-lived cool season grass common to the Intermountain Region of the Western USA and grows from 40 to 120 cm tall. Achnatherum hymenoides (Indian ricegrass) is adapted to sand-textured soils, is drought-tolerant, and ranges from 5 to 75 cm tall. Leymus triticoides (creeping wild rye) is a rhizomatous grass common to moist soils and can reach over 1 m in height.

Further experimental protocols are summarized in Table 1. Two seeds of each grass were sown in the rhizotrons 6 cm from each edge to leave an 18 cm space between for planting of B. tectorum. During initial establishment, perennial grasses were supplemented with 500 to 1000 mL of deionized water per week. The experiment was continued for five separate B. tectorum growth cycles (Table 1). Additionally, for each growth cycle four replicate rhizotrons were sown to just B. tectorum to serve as control and thereby gage the influence of established perennial grasses on B. tectorum growth through time. Supplemental lighting, using 4 high pressure sodium lamps each producing 124,000 lumens at 2,100°K temperature, was used to assure at least 12 hours of daylight. For each harvest, above-ground tissue was dried for 48 hrs at 70°C, weight recorded and reserved for nutrient analyses. Following each harvest, B. tectorum roots were left undisturbed except in preparation for the 3rd growth cycle (Table 1). Through the experiment, deionized water was added to the soil surface twice weekly amounting to between 300 to 1000 mL depending on visual indication of soil moisture content as viewed through the plastic rhizotron backs. Additionally, small amounts of water were added as needed in the immediate vicinity of the competed B. tectorum to assure water availability—water was not limiting in this study. Following final harvest, using a 2.5 cm diameter-coring device, soil was collected at depths between 0–30 and 30–60 cm directly beneath perennial grasses and directly beneath B. tectorum, both with or without competition. For these soil samples and original soil before planting: (1) phosphorus in the soil solution was extracted using immiscible displacement [37] and quantified by ion chromatography; (2) the mineral nitrogen pool was extracted with KCl [38] and and quantified by flow-injection methodology (Lachat); (3) the bicarbonate-extractable phosphorus pool was quantified using the Olsen method [39] with quantification using molybdenum-blue colorimetry; (4) total nitrogen and carbon were quantified by Dumas combustion using a Leco analyzer. Total nitrogen in plant tissue was quantified by Dumas combustion using a LECO analyzer. Phosphorus in plant tissue was determined using a dry ash procedure with solubilization in 1 N HCl [40] followed by quantification using vanadomolybdate chemistry. Standards were NIST-(National Institute of Standards and Technology) certified, and NIST-certified reference plant tissue was used as a check.

tab1
Table 1: Summary and time line of experimental protocols.

The data structure is 3 perennial grass species in competition with B. tectorum replicated 4 times for a total of 12 rhizotrons plus 4 replicates of B. tectorum grown without competition. Given changing greenhouse conditions over the five growth cycles, it is not justified to compare between growth cycles for individual attributes. Therefore, a separate ANOVA was run for each growth cycle to compare between above-ground biomasses and tissue nutrient concentrations, with Tukey’s Honest Significant difference as a post hoc test. As an index of changing plant biomass over the five growth cycles, for each growth cycle, a ratio of the average of above-ground biomass between B. tectorum without competition to that of competed B. tectorum above-ground biomass was computed. ANOVA was used to analyze soil data after the 5th harvest with categorical variables PLANT (beneath perennial grasses, beneath competed B. tectorum, and beneath B. tectorum without competition) and DEPTH (0–30 and 30–60 cm). Tukey’s was also used as a post hoc test. Before ANOVAs were run, data were normalized as necessary using square root or log transformations.

3. Results

3.1. Soil and Plant Growth

Throughout the Intermountain West of the United States, healthy, established perennial grass communities suppress annual weeds including B. tectorum (Figure 1). We investigated mechanisms involved in the suppression of B. tectorum in the greenhouse (Figure 1). The soil used in this experiment is low in total carbon and nitrogen, typical of an arid land soil (Table 2). This low carbon/nitrogen ratio indicates the potential to mineralize organic-bound nitrogen. Levels of phosphorus in the soil-solution pool and bicarbonate-extractable pool, as well as mineral nitrogen, indicated that the soil is relatively infertile. Using this soil, established perennial grasses significantly suppressed B. tectorum growth, but the magnitude depended on growth cycle and the competing perennial species (Tables 3 and 4). In absolute terms, biomass of B. tectorum in competition increased with each growth cycle. Clipped biomass of the perennial grasses and B. tectorum without competition generally declined with growth cycle, but all increased biomass after the 4th growth cycle (fertilizer addition). All the tested perennial species suppressed B. tectorum, but for most growth cycles, suppression was least between A. hymenoides. Greatest suppression of B. tectorum occurred after the 1st growth cycle, where its above-ground biomass averaged 3480 times less than B. tectorum grown without competition. The above-ground biomass ratio of B. tectorum without competition to B. tectorum in competition decreased with each growth cycle, but the greatest relative decrease occurred after the perennial plants were killed (5th growth cycle).

tab2
Table 2: Selected attributes of the soil before planting.
tab3
Table 3: Mean above-ground biomass (g) by plant species and growth cycle.
tab4
Table 4: Above-ground biomass ratios of B. tectorum grown without competition (WC) to B. tectorum grown in competition (IC), by growth cycle.
fig1
Figure 1: (a) was taken in the Virginia Range of northern Nevada, USA. These high elevation communities are dominated by the low sagebrush species Artemisia arbuscula due to the clay-textured soils. The trees are Juniperus occidentalis that are greatly expanding their range. The grass in the foreground is the native perennial bunchgrass Psuedoreogneria spicata, which effectively suppresses growth of Bromus tectorum. The vegetation in the background is dominated by B. tectorum, which we suspect is due to loss of P. spicata. (b) shows a rhizotron used in the greenhouse experiment with the back removed to observe rooting patterns. Photograph was taken near the completion of the 3rd growth cycle (addition of activated carbon) and shows the perennial grass A. hymenoides with a small plant of B. tectorum between.
3.2. Tissue Nutrient Concentrations and Uptake of Nitrogen and Phosphorus

Tissue nitrogen concentrations varied among the tested plant species and growth cycles (Table 5). For the first two growth cycles, tissue nitrogen in B. tectorum without competition was significantly greater than tissue nitrogen of perennial grasses and far greater than that of B. tectorum in competition. All perennial grasses and B. tectorum in competition had much greater tissue nitrogen after the 3rd growth cycle; indeed approaching that of B. tectorum without competition. Noteworthy are the high tissue nitrogen levels for A. hymenoides, known to fix nitrogen in its rhizosphere [41], after the 3rd cycle. Following fertilizer top-dressing (4th cycle), B. tectorum grown with and without competition appeared to utilize added nitrogen judging from the large increase in tissue nitrogen. Likewise, it seems that L. triticoides utilized the fertilizer nitrogen; however, E. wawawaensis and A. hymenoides did not.

tab5
Table 5: Mean above-ground tissue nitrogen and phosphorus concentrations by plant species and growth cycle.

In almost all instances, B. tectorum had significantly greater tissue phosphorus concentrations than the perennial grasses (Table 5). Bromus tectorum, both in and without competition, had statistically similar tissue phosphorus concentrations after the 3rd and 4th growth cycles; however, after the 5th growth cycle (perennials killed), the formerly competed B. tectorum had statistically greater tissue phosphorus concentrations. For the perennial grasses, tissue phosphorus increased from the 1st to the 3rd growth cycles (A. hymenoides declined in the 2nd), and then declined in the 4th growth cycle.

Over the first four growth cycles, B. tectorum grown without competition had far greater uptake of nitrogen and phosphorus than the perennial grasses (Figure 2). It was not until the 5th growth cycle (perennials killed) that B. tectorum in competition uptook sizeable levels of nitrogen or phosphorus.

fig2
Figure 2: Graphs showing cumulative plant uptake of nitrogen and phosphorus by growth cycle.
3.3. Soil Nutrients Following Final Harvest

Following the 5th growth cycle, soil nutrient pools were quantified (Table 6). Mineral nitrogen pools exceeded the initial soil values (Table 1) at all depths and microsites, which is likely due to fertilizer additions during the 4th growth cycle. Mineral nitrogen in the soil beneath competed B. tectorum is statistically similar to that beneath B. tectorum grown without competition. The lowest mineral nitrogen pool occurred beneath the surface 30 cm of perennial grasses. The molar proportion of in the mineral nitrogen pool was statistically greater in the surface 30 cm beneath competed B. tectorum and the perennial grasses. The soil solution P pool was statistically similar among microsites. Values of phosphorus for the surface 30 cm are similar to initial values of the soil (Table 1), but phosphorus values for the 30–60 cm depth increment were statistically lower.

tab6
Table 6: Selected soil nutrient measurements following the 5th harvest.

4. Discussion

Established perennial grasses significantly suppressed the growth of B. tectorum, thus supporting our first hypothesis. The magnitude of suppression was remarkable in the 1st and 2nd growth cycles; B. tectorum never produced more than 3 leaves after 70 days of growth. By comparison, B. tectorum grown without competition produced hundreds of leaves during the same periods. Water availability can be a key determinant in the competitive ability of B. tectorum [42]; however, in this study, growth suppression is not due to water limitation as plants were frequently supplemented with water. What then are the mechanistic underpinnings for suppression of B. tectorum? Resistance to invasion is exceedingly complex, an interaction of various biotic and abiotic factors in the host soil environment [43].

In our study, growth of B. tectorum in competition increased minimally from the 1st to 2nd growth cycles, slightly more after the 3rd growth cycle (activated carbon addition), sizably after the 4th growth cycle (fertilizer addition), and greatly after the 5th growth cycle (perennial death). When one compares the ratio between B. tectorum grown without competition and plants in competition over the five growth cycles, a different picture emerges. From the 1st through 3rd growth cycles, this ratio declined precipitously. Fertilizer addition (4th cycle) resulted in greater relative growth of controls. It is only after the death of perennials (5th growth cycle) that competed B. tectorum vastly increased its growth relative the controls. These data suggest that a combination of reduced nitrogen availability and coopting of biological soil space may be responsible for suppression of B. tectorum by established perennial grasses. Our data do not allow acceptance or rejection of allelopathy as a mechanism in suppression.

The first mechanism our data supports is that established perennial grasses reduced the availability of nitrogen (possibly phosphorus) in the soil of establishing B. tectorum plants, thus supporting our second hypothesis. Prober and Lunt [35] reported that the native perennial grass Themeda australis reduced soil and thereby decreased invasion by nitrophilic annuals. Evidence for a similar mechanism operating in this study included lower tissue nitrogen concentrations for the 1st and 2nd growth cycles for B. tectorum in competition, relative to B. tectorum grown without competition (Table 5) and the increase in absolute growth and tissue nitrogen concentrations of B. tectorum in competition after fertilizer addition. Bromus tectorum is a nitophile, and its growth and competitive ability is increased as nitrogen availability is elevated [21, 44, 45] and lowered resource availability has been suggested as to why some plant communities are resistant to B. tectorum invasion [15]. It is by no means clear, however, that lowered soil nitrogen availability can by itself completely assure that B. tectorum cannot invade particular sites [43]. Due to lack of sufficient sample we could not quantify phosphorus in B. tectorum in competition for the 1st and 2nd growth cycles. It is possible that like nitrogen, phosphorus was less available. Gundale et al. [23] determined that soil beneath perennial bunchgrasses was phosphorus-limited and negatively affected the growth of B. tectorum.

An aspect of mineral nitrogen, other than its availability, may influence the suppression of B. tectorum. Surface soil beneath the perennial grasses and competed B. tectorum has a significantly greater proportion of mineral N in the form compared to B. tectorum grown without competition (Table 6). Empirical evidence has shown that B. tectorum has greater uptake kinetics for nitrogen in the form rather than the form [46]. Indeed, B. tectorum-occupied soils have elevated nitrification rates, relative to native ecosystems, such that a greater proportion of mineral nitrogen is in the form [42]. In a well-established and healthy stand of the perennial grass Agropyron cristatum in northern Nevada, which resists invasion by B. tectorum, the molar proportion of in the mineral N fraction often exceeds 90% [47]. We conjecture that a portion of perennial grass suppression of B. tectorum growth in the present study may be due to inhibited nitrification, which reduces the availability of . In a west African shrub savannah, grasses have been shown to inhibit soil nitrification [48]. Data from our experimental treatments, at least initially, argue against nitrification inhibition as a major factor in the suppression of B. tectorum. Allelochemicals are often implicated in nitrification inhibition [49]; yet, the activated carbon treatment (3rd growth cycle), which can ameliorate allelopathic activity [50], caused very little increase in the growth of B. tectorum in competition. The veracity of our inferences that activated carbon ameliorates allelopathy must be questioned based on recent research [51, 52]. A more persuasive argument that nitrification inhibition may not have a major role in suppression is that application of large quantities of (4th growth cycle) did significantly increase B. tectorum above-ground biomass grown in competition relative to above-ground biomass of B. tectorum grown without competition.

Death of competing perennial grasses (5th growth cycle) greatly released the growth potential of B. tectorum. What aspects of the death of a competing plant might so affect the growth of B. tectorum? Established perennials may reduce light resources to B. tectorum; however, the spacing afforded in this rhizotron experiment and perennial grass clipping argues against any light limitation. Water resources could be so depleted by the established perennial grasses such that newly added seeds of B. tectorum could not attain maximum growth. Again, as stated earlier, the competing B. tectorum plants in this study were given adequate water. Death of plant roots can provide nutrients to new plants [53] and thereby facilitate the growth of B. tectorum. We doubt, however, that this process could so increase the growth of B. tectorum for two reasons. Firstly, B. tectorum grown in competition did not greatly respond to fertilizer top-dressing relative to its increase at perennial plant death. Secondly, the cumulative total plant uptake of nitrogen and phosphorus over the first four growth cycles was far greater for B. tectorum growth without competition than the perennial grasses (Figure 1). This fact suggests that, even after four growth cycles, soil beneath perennial grasses had nutrient availability that was adequate to support very high growth of B. tectorum grown in competition.

We believe that our data supports a part of hypothesis three, that established perennial grass roots occupy biological soil space and/or exuded allelopathies, thus causing reduction in the growth potential of B. tectorum. A recent review essay has presented a compelling case that root competition is far more complex than just resource depletion [28]. By occupying biological space, intact perennial roots can alter the architecture and activity of an invading root [31]. Plants can sense neighboring roots via chemical signaling (allelochemicals) and adjust growth patterns accordingly [49]. We believe that a portion of the growth reduction seen in competed B. tectorum may be due to its sensing of soil occupied by perennial roots. From the seedling stage, roots of B. tectorum seem unaffected by perennial grass neighbors, indeed they intermingle and likely coopt space and nutrients [14]. Clearly, established perennial grass roots are able to suppress root growth of B. tectorum as indicated by its lack of rooting in the rhizotrons. By what specific mechanism(s) might occupation of biological space affect root suppression? Unfortunately, specific mechanisms of how biological soil space influences plant growth remain elusive [31]. A reasonable inference based on our research is that established perennial roots simply interfere with the expansion of roots of B. tectorum. Due to the limitations of activated carbon in allelopathic research [51, 52], we cannot state with confidence that the perennial grasses exuded allelopathies, which suppressed B. tectorum. Published literature, however, reports that allelopathies, exuded from native flora, assist in the resistance to invasive plants [35].

5. Conclusions

Established perennial grasses greatly suppress the growth of B. tectorum. Our research hints at causative mechanisms including reduced nutrient availability and coopting of biological soil space; unfortunately, the definitive mechanisms have not been identified. Understanding the suppressive nature of established perennial grasses on growth of B. tectorum may lead to greater success in rehabilitation of native plant communities invaded by B. tectorum. Future studies should attempt to design appropriate experiments to tease out the role of biological soil space in suppression.

Disclosure

Any mention of a proprietary product does not constitute a guarantee or warranty of the product by USDA or the authors and does not imply its approval to the exclusion of the other products that also may be suitable.

References

  1. M. A. Bradley and J. F. Mustard, “Identifying land cover variability distinct from land cover change: cheatgrass in the Great Basin,” Remote Sensing of Environment, vol. 94, no. 2, pp. 204–213, 2005. View at Publisher · View at Google Scholar · View at Scopus
  2. E. L. Rice, “Allelopathic effect on nitrogen cycling,” in Allelopathy: Basic and Applied Aspects, pp. 31–58, Chapman & Hall, London, UK, 1992.
  3. C. M. D'Antonio and P. M. Vitousek, “Biological invasions by exotic grasses, the grass/fire cycle, and global change,” Annual Review of Ecology and Systematics, vol. 23, no. 1, pp. 63–87, 1992. View at Scopus
  4. G. A. Harris, “Some competitive relationships between Agropyron spicatum and Bromus tectorum,” Ecological Monographs, vol. 37, pp. 89–111, 1967. View at Publisher · View at Google Scholar
  5. G. A. Harris, “Root phenology as a factor of competition among grass seedlings,” Journal of Range Management, vol. 30, pp. 172–177, 1977. View at Publisher · View at Google Scholar
  6. G. S. Stewart and A. C. Hull, “Cheatgrass (Bromus tectorum L.)—an ecologic intruder in southern Idaho,” Ecology, vol. 30, pp. 58–74, 1949.
  7. R. F. Daubenmire, “An ecological study of the vegetation of southeastern Washington and adjacent Idaho,” Ecological Monographs, vol. 12, pp. 53–79, 1942. View at Publisher · View at Google Scholar
  8. J. O. Klemmedson and J. G. Smith, “Cheatgrass (Bromus tectorum L.),” Botanical Review, vol. 30, pp. 226–262, 1964. View at Publisher · View at Google Scholar
  9. R. L. Piemeisel, “Causes affecting change and rate of change in a vegetation of annuals in Idaho,” Ecology, vol. 32, pp. 53–72, 1951. View at Publisher · View at Google Scholar
  10. S. D. Smith, T. E. Huxman, S. F. Zitzer et al., “Elevated CO2 increases productivity and invasive species success in an arid ecosystem,” Nature, vol. 408, no. 6808, pp. 79–82, 2000. View at Publisher · View at Google Scholar · View at Scopus
  11. L. H. Ziska, J. B. Reeves III, and B. Blank, “The impact of recent increases in atmospheric CO2 on biomass production and vegetative retention of Cheatgrass (Bromus tectorum): implications for fire disturbance,” Global Change Biology, vol. 11, no. 8, pp. 1325–1332, 2005. View at Publisher · View at Google Scholar · View at Scopus
  12. R. S. Rummell, “Some effects of competition from cheatgrass brome on crested wheatgrass and bluestem wheatgrass,” Ecology, vol. 27, pp. 159–167, 1946. View at Publisher · View at Google Scholar
  13. M. G. Francis and D. A. Pyke, “Crested wheatgrass-cheatgrass seedling competition in a mixed-density design,” Journal of Range Management, vol. 49, no. 5, pp. 432–438, 1996. View at Scopus
  14. R. R. Blank, “Intraspecific and interspecific pair-wise seedling competition between exotic annual grasses and native perennials: plant-soil relationships,” Plant and Soil, vol. 326, no. 1, pp. 331–343, 2010. View at Publisher · View at Google Scholar · View at Scopus
  15. C. M. D'Antonio and M. Thomsen, “Ecological resistance in theory and practice,” Weed Technology, vol. 18, no. 1, pp. 1572–1577, 2004. View at Publisher · View at Google Scholar · View at Scopus
  16. J. Beckstead and C. K. Augspurger, “An experimental test of resistance to cheatgrass invasion: limiting resources at different life stages,” Biological Invasions, vol. 6, no. 4, pp. 417–432, 2004. View at Publisher · View at Google Scholar · View at Scopus
  17. J. C. Chambers, B. A. Roundy, R. R. Blank, S. E. Meyer, and A. Whittaker, “What makes Great Basin sagebrush ecosystems invasible by Bromus tectorum,” Ecological Monographs, vol. 77, no. 1, pp. 117–145, 2007. View at Publisher · View at Google Scholar · View at Scopus
  18. L. D. Humphrey and E. W. Schupp, “Competition as a barrier to establishment of a native perennial grass (Elymus elymoides) in alien annual grass (Bromus tectorum) communities,” Journal of Arid Environments, vol. 58, no. 4, pp. 405–422, 2004. View at Publisher · View at Google Scholar · View at Scopus
  19. M. M. Borman, W. C. Krueger, and D. E. Johnson, “Effects of established perennial grasses on yields of associated annual weeds,” Journal of Range Management, vol. 44, no. 4, pp. 318–322, 1991. View at Scopus
  20. C. G. Elton, The Ecology of Invasions by Animals and Plants, Methuen, London, UK, 1958.
  21. E. C. Adair, I. C. Burke, and W. C. Lauenroth, “Contrasting effects of resource availability and plant mortality on plant community invasion by Bromus tectorum L.,” Plant and Soil, vol. 304, no. 1-2, pp. 103–115, 2008. View at Publisher · View at Google Scholar · View at Scopus
  22. M. S. Booth, M. M. Caldwell, and J. M. Stark, “Overlapping resource use in three Great Basin species: implications for community invasibility and vegetation dynamics,” Journal of Ecology, vol. 91, no. 1, pp. 36–48, 2003. View at Publisher · View at Google Scholar · View at Scopus
  23. M. J. Gundale, S. Sutherland, and T. H. DeLuca, “Fire, native species, and soil resource interactions influence the spatio-temporal invasion pattern of Bromus tectorum,” Ecography, vol. 31, no. 2, pp. 201–210, 2008. View at Publisher · View at Google Scholar · View at Scopus
  24. B. L. Kay and R. A. Evans, “Effects of fertilization on a mixed stand of cheatgrass and intermediate wheatgrass,” Journal of Range Management, vol. 18, pp. 7–11, 1965. View at Publisher · View at Google Scholar
  25. M. W. Paschke, T. McLendon, and E. F. Redente, “Nitrogen availability and old-field succession in a shortgrass steppe,” Ecosystems, vol. 3, no. 2, pp. 144–158, 2000. View at Publisher · View at Google Scholar · View at Scopus
  26. H. I. Rowe, C. S. Brown, and M. W. Paschke, “The influence of soil inoculum and nitrogen availability on restoration of high-elevation steppe communities invaded by Bromus tectorum,” Restoration Ecology, vol. 17, no. 5, pp. 686–694, 2009. View at Publisher · View at Google Scholar · View at Scopus
  27. R. R. Blank and J. A. Young, “Plant-soil relationships of Bromus tectorum L.: interactions among labile carbon additions, soil invasion status, and fertilizer,” Applied and Environmental Soil Science, vol. 2009, Article ID 929120, 7 pages, 2009.
  28. B. B. Casper and R. B. Jackson, “Plant competition underground,” Annual Review of Ecology and Systematics, vol. 28, pp. 545–570, 1997. View at Publisher · View at Google Scholar · View at Scopus
  29. H. J. Schenk, “Root competition: beyond resource depletion,” Journal of Ecology, vol. 94, no. 4, pp. 725–739, 2006. View at Publisher · View at Google Scholar · View at Scopus
  30. M. A. Ross and J. L. Harper, “Occupation of biological space during seedling establishment,” Journal of Ecology, vol. 60, pp. 77–88, 1972. View at Publisher · View at Google Scholar
  31. K. D. M. McConnaughay and F. A. Bazzaz, “Is physical space a soil resource?” Ecology, vol. 72, no. 1, pp. 94–103, 1991. View at Scopus
  32. K. D. M. McConnaughay and F. A. Bazzaz, “The occupation and fragmentation of space: consequences of neighbouring roots,” Functional Ecology, vol. 6, no. 6, pp. 704–710, 1992. View at Scopus
  33. R. M. Callaway and J. L. Hierro, “Resistance and susceptibility of plant communities to invasion: revisiting rabotnov’s ideas about community homeostasis,” in Alleolpathy: A Physiological Process With Ecological Implications, pp. 395–414, Springer, Amsterdam, The Netherlands, 2006.
  34. A. S. Kumar H. P. Bias, “Allelopathy and exotic plant invasion,” in Plant Communication from an Ecological Perspective, Signaling and Communication in Plants, pp. 61–73, Springer, Berlin, Germany, 2010.
  35. S. M. Prober and I. D. Lunt, “Restoration of Themeda australis swards suppresses soil nitrate and enhances ecological resistance to invasion by exotic annuals,” Biological Invasions, vol. 11, no. 2, pp. 171–181, 2009. View at Publisher · View at Google Scholar · View at Scopus
  36. J. D. Weidenhamer J. T. Romeo, “Allelopathy as a mechanism for resisting invasion: the case of Polygonella myriophylla,” in Invasive Plants: Ecological and Agricultural Aspects, pp. 167–177, Birkhäuser Verlang, Basel, Switzerland, 2005.
  37. A. Mubarek and R. A. Olsen, “Immiscible displacement of the soil solution by centrifugation,” Soil Science Society of America Journal, vol. 40, pp. 329–331, 1976.
  38. D. R. Keeney and D. W. Nelson, “Nitrogen—inorganic forms,” in Methods of Soil Analysis, Part 2. Chemical and Microbiological Properties, pp. 643–698, American Society of Agronomy, Madison, Wis, USA, 1982.
  39. S. R. Olsen and L. E. Sommers, “Phosphorus,” in Methods of Soil Analysis, Part 2. Chemical and Microbiological PropertiesAmerican Society of Agronomy, pp. 403–430, American Society of Agronomy, Madison, Wis, USA, 1982.
  40. Y. P. Kalra, Handbook of Reference Methods for Plant Analysis, CRC Press, Boca Raton, Fla, USA, 1998.
  41. L. H. Wullstein, M. L. Bruening, and W. B. Bollen, “Nitrogen fixation associated with sand grain root sheaths (rhizosheaths) of certain xeric grasses,” Physiologia Plantarum, vol. 46, pp. 1–4, 1979. View at Publisher · View at Google Scholar
  42. M. S. Booth, J. M. Stark, and M. M. Caldwell, “Inorganic N turnover and availability in annual- and perennial-dominated soils in a northern Utah shrub-steppe ecosystem,” Biogeochemistry, vol. 66, no. 3, pp. 311–330, 2003. View at Publisher · View at Google Scholar · View at Scopus
  43. C. M. D'Antonio and M. Thomsen, “Ecological resistance in theory and practice,” Weed Technology, vol. 18, no. 1, pp. 1572–1577, 2004. View at Publisher · View at Google Scholar · View at Scopus
  44. E. Vasquez, R. Sheley, and T. Svejcar, “Nitrogen enhances the competitive ability of cheatgrass (Bromus tectotum) relative to native grasses,” Invasive Plant Science and Management, vol. 1, no. 3, pp. 287–295, 2008. View at Publisher · View at Google Scholar · View at Scopus
  45. J. J. James, “Effect of soil nitrogen stress on the relative growth rate of annual and perennial grasses in the Intermountain West,” Plant and Soil, vol. 310, no. 1-2, pp. 201–210, 2008. View at Publisher · View at Google Scholar · View at Scopus
  46. C. T. MacKown, T. A. Jones, D. A. Johnson, T. A. Monaco, and M. G. Redinbaugh, “Nitrogen uptake by perennial and invasive annual grass seedlings: nitrogen form effects,” Soil Science Society of America Journal, vol. 73, no. 6, pp. 1864–1870, 2009. View at Publisher · View at Google Scholar · View at Scopus
  47. R. R. Blank and T. Morgan, “Mineral nitrogen in a crested wheatgrass stand: implications for suppression of cheatgrass,” Rangeland Ecology and Management, vol. 65, pp. 101–104, 2012. View at Publisher · View at Google Scholar
  48. J. C. Lata, V. Degrange, X. Raynaud, P. A. Maron, R. Lensi, and L. Abbadie, “Grass populations control nitrification in savanna soils,” Functional Ecology, vol. 18, no. 4, pp. 605–611, 2004. View at Publisher · View at Google Scholar · View at Scopus
  49. E. L. Rice and S. K. Pancholy, “Inhibition of nitrification by climax ecosystem. III. Inhibitors other than tannins,” American Journal of Botany, vol. 61, pp. 1095–1103, 1991.
  50. J. Q. Yu and Y. Matsui, “Phytotoxic substances in root exudates of cucumber (Cucumis sativus L.),” Journal of Chemical Ecology, vol. 20, no. 1, pp. 21–31, 1994. View at Scopus
  51. J. A. Lau, K. P. Puliafico, J. A. Kopshever et al., “Inference of allelopathy is complicated by effects of activated carbon on plant growth,” New Phytologist, vol. 178, no. 2, pp. 412–423, 2008. View at Publisher · View at Google Scholar · View at Scopus
  52. K. Weißhuhn and D. Prati, “Activated carbon may have undesired side effects for testing allelopathy in invasive plants,” Basic and Applied Ecology, vol. 10, no. 6, pp. 500–507, 2009. View at Publisher · View at Google Scholar · View at Scopus
  53. W. S. Gordon and R. B. Jackson, “Nutrient concentrations in fine roots,” Ecology, vol. 81, no. 1, pp. 275–280, 2000.